UREMOL HC
UREMOL HC
Discontinued
DIN Number
00560022
Drug Class
Human
Market Date
Dec 31, 1983
Company
HC
GlaxoSmithKline Inc
Product Information
Detailed information about this Health Canada approved drug product, including dosage form, route of administration, and regulatory classification.
Product Details
Health Canada regulatory and product classification information
Regulatory Identifiers
DIN Number00560022
AIG Number0231440001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
D07XA01 HYDROCORTISONE
Product Specifications
Dosage FormLotion
Route of AdministrationTopical
AHFS Classification84:28.00
Health Canada Classification
ACTIVE INGREDIENTS (2)
HYDROCORTISONE ACETATEActive
Strength: 1 %
Monograph: HYDROCORTISONE ACETATE
UREAActive
Strength: 10 %
Monograph: UREA